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Acetaldehyde → 2-[N-(Methylmethylene)amino]-4methylpentanoic acid, tert-butyl ester

HRID 854341
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HRID 854341 반응식
[C:1]([O:5][C:6](=[O:13])[C@H:7]([CH2:9][CH:10]([CH3:12])[CH3:11])[NH2:8])([CH3:4])([CH3:3])[CH3:2].[CH:14](=O)[CH3:15].S([O-])([O-])(=O)=O.[Na+].[Na+]>>[CH3:14][CH:15]=[N:8][CH:7]([CH2:9][CH:10]([CH3:11])[CH3:12])[C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 177AcetaldehydeHCID 24436Sodium SulfateHCID 7022311tert-butyl (2S)-2-amino-4-methylpentanoate

생성물 1

HCID 589340072-[N-(Methylmethylene)amino]-4methylpentanoic acid, tert-butyl ester

실험 절차

A solution of leucine tert-butyl ester (2.0 g, 8.9 mmol) and acetaldehyde (999 ul, 17.9 mmol) was stirred at room temperature for 5 minutes. Anhydrous sodium sulphate was added and the mixture stirred at room temperature for 18 hours. The solid was removed by filtration and the solvent evaporated in vacuo to afford the title compound as an oil.

후처리

  1. customThe solid was removed by filtration
  2. customthe solvent evaporated in vacuo

출처 및 근거

ORD 기록
ord-948466db67134022aee4612d43eca131
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07259163B2

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